Trial · NCT07506044
Dexmedetomidine as an Adjuvant During Dural Puncture Epidural
NCT07506044, Not applicable, Recruiting, Menoufia University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Dexmedetomidine as an Adjuvant During Dural Puncture Epidural. Trials, record NCT07506044. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07506044
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Dexmedetomidine as an Adjuvant During Dural Puncture Epidural
- NCT number
- NCT07506044
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 140 participants, estimated
- Lead sponsor
- Menoufia University
- Conditions
- Total Dose of Bupivacaine Administered During Labor
- Interventions
- Epidural Catheter with bupivacaine, Epidural with dural puncture, Dexmedetomidine 0.4 added, Dexmedetomidine 0.6 added
- First posted
- 2026-04-01
- Last updated
- 2026-08-13
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Total dose of bupivacaine | From the induction of epidural to the delivery of the fetus | Total dose of bupivacaine administered |
| Secondary | Labor pain | Before initiation of epidural ,10 ,30,45,60 min after initiation then every 1hour till the delivery of the fetus | Labour pain measured by Visual analogue |
| Secondary | Motor block | Before initiation of epidural ,10 ,30,45,60 min after initiation then every 1hour till the delivery of the fetus | Motor block measured by bromage scsle |
| Secondary | Delivery type | At time of fetus delivery | Delivery type spontaneous or instrument |
| Secondary | Maternal satisfaction | Preoperative,2nd stage of labour, third stage of labour and immediately after delivery, 2 hours after delivery,4 hours after delivery,12 hours after delivery | Satisfied or not |
| Secondary | Complications | Preoperative,2nd stage of labour, third stage of labour and immediately after delivery, 2 hours after delivery,4 hours after delivery,12 hours after delivery | Any complications detected |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07506044
GET https://conductscience.org/api/trials/v1/NCT07506044/registered